Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

97 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Publication Date timeline is not available.
Page 1
Effects of complement gene-set polygenic risk score on brain volume and cortical measures in patients with psychotic disorders and healthy controls.
Holland JF, Cosgrove D, Whitton L, Harold D, Corvin A, Gill M, Mothersill DO, Morris DW, Donohoe G. Holland JF, et al. Among authors: harold d. Am J Med Genet B Neuropsychiatr Genet. 2020 Dec;183(8):445-453. doi: 10.1002/ajmg.b.32820. Epub 2020 Sep 12. Am J Med Genet B Neuropsychiatr Genet. 2020. PMID: 32918526
MiR-137-derived polygenic risk: effects on cognitive performance in patients with schizophrenia and controls.
Cosgrove D, Harold D, Mothersill O, Anney R, Hill MJ, Bray NJ, Blokland G, Petryshen T; Wellcome Trust Case Control Consortium; Richards A, Mantripragada K, Owen M, O'Donovan MC, Gill M, Corvin A, Morris DW, Donohoe G. Cosgrove D, et al. Among authors: harold d. Transl Psychiatry. 2017 Jan 24;7(1):e1012. doi: 10.1038/tp.2016.286. Transl Psychiatry. 2017. PMID: 28117840 Free PMC article.
Cognitive analysis of schizophrenia risk genes that function as epigenetic regulators of gene expression.
Whitton L, Cosgrove D, Clarkson C, Harold D, Kendall K, Richards A, Mantripragada K, Owen MJ, O'Donovan MC, Walters J, Hartmann A, Konte B, Rujescu D; WTCCC2; Gill M, Corvin A, Rea S, Donohoe G, Morris DW. Whitton L, et al. Among authors: harold d. Am J Med Genet B Neuropsychiatr Genet. 2016 Dec;171(8):1170-1179. doi: 10.1002/ajmg.b.32503. Epub 2016 Oct 20. Am J Med Genet B Neuropsychiatr Genet. 2016. PMID: 27762073
Cognitive Characterization of Schizophrenia Risk Variants Involved in Synaptic Transmission: Evidence of CACNA1C's Role in Working Memory.
Cosgrove D, Mothersill O, Kendall K, Konte B, Harold D, Giegling I, Hartmann A, Richards A, Mantripragada K; Wellcome Trust Case Control Consortium; Owen MJ, O'Donovan MC, Gill M, Rujescu D, Walters J, Corvin A, Morris DW, Donohoe G. Cosgrove D, et al. Among authors: harold d. Neuropsychopharmacology. 2017 Dec;42(13):2612-2622. doi: 10.1038/npp.2017.123. Epub 2017 Jun 13. Neuropsychopharmacology. 2017. PMID: 28607492 Free PMC article.
Effects of MiR-137 genetic risk score on brain volume and cortical measures in patients with schizophrenia and controls.
Cosgrove D, Mothersill DO, Whitton L, Harold D, Kelly S, Holleran L, Holland J, Anney R; Wellcome Trust Case Control Consortium; Richards A, Mantripragada K, Owen M, O'Donovan MC, Gill M, Corvin A, Morris DW, Donohoe G. Cosgrove D, et al. Among authors: harold d. Am J Med Genet B Neuropsychiatr Genet. 2018 Apr;177(3):369-376. doi: 10.1002/ajmg.b.32620. Epub 2018 Feb 8. Am J Med Genet B Neuropsychiatr Genet. 2018. PMID: 29418072
Population-based identity-by-descent mapping combined with exome sequencing to detect rare risk variants for schizophrenia.
Harold D, Connolly S, Riley BP, Kendler KS, McCarthy SE, McCombie WR, Richards A, Owen MJ, O'Donovan MC, Walters J; Wellcome Trust Case Control Consortium 2; Schizophrenia Working Group of the Psychiatric Genomics Consortium; Donohoe G, Gill M, Corvin A, Morris DW. Harold D, et al. Am J Med Genet B Neuropsychiatr Genet. 2019 Apr;180(3):223-231. doi: 10.1002/ajmg.b.32716. Epub 2019 Feb 23. Am J Med Genet B Neuropsychiatr Genet. 2019. PMID: 30801977 Free PMC article.
Analysis of shared heritability in common disorders of the brain.
Brainstorm Consortium; Anttila V, Bulik-Sullivan B, Finucane HK, Walters RK, Bras J, Duncan L, Escott-Price V, Falcone GJ, Gormley P, Malik R, Patsopoulos NA, Ripke S, Wei Z, Yu D, Lee PH, Turley P, Grenier-Boley B, Chouraki V, Kamatani Y, Berr C, Letenneur L, Hannequin D, Amouyel P, Boland A, Deleuze JF, Duron E, Vardarajan BN, Reitz C, Goate AM, Huentelman MJ, Kamboh MI, Larson EB, Rogaeva E, St George-Hyslop P, Hakonarson H, Kukull WA, Farrer LA, Barnes LL, Beach TG, Demirci FY, Head E, Hulette CM, Jicha GA, Kauwe JSK, Kaye JA, Leverenz JB, Levey AI, Lieberman AP, Pankratz VS, Poon WW, Quinn JF, Saykin AJ, Schneider LS, Smith AG, Sonnen JA, Stern RA, Van Deerlin VM, Van Eldik LJ, Harold D, Russo G, Rubinsztein DC, Bayer A, Tsolaki M, Proitsi P, Fox NC, Hampel H, Owen MJ, Mead S, Passmore P, Morgan K, Nöthen MM, Rossor M, Lupton MK, Hoffmann P, Kornhuber J, Lawlor B, McQuillin A, Al-Chalabi A, Bis JC, Ruiz A, Boada M, Seshadri S, Beiser A, Rice K, van der Lee SJ, De Jager PL, Geschwind DH, Riemenschneider M, Riedel-Heller S, Rotter JI, Ransmayr G, Hyman BT, Cruchaga C, Alegret M, Winsvold B, Palta P, Farh KH, Cuenca-Leon E, Furlotte N, Kurth T, Ligthart L, Terwindt GM, Fr… See abstract for full author list ➔ Brainstorm Consortium, et al. Among authors: harold d. Science. 2018 Jun 22;360(6395):eaap8757. doi: 10.1126/science.aap8757. Science. 2018. PMID: 29930110 Free PMC article.
Identifying schizophrenia patients who carry pathogenic genetic copy number variants using standard clinical assessment: retrospective cohort study.
Foley C, Heron EA, Harold D, Walters J, Owen M, O'Donovan M, Sebat J, Kelleher E, Mooney C, Durand A, Pinto C, Cormican P, Morris D, Donohoe G, Gill M, Gallagher L, Corvin A. Foley C, et al. Among authors: harold d. Br J Psychiatry. 2020 May;216(5):275-279. doi: 10.1192/bjp.2019.262. Br J Psychiatry. 2020. PMID: 31964429
97 results